Label: LIDOZEN- lidocaine, menthol patch
- NDC Code(s): 71574-900-05
- Packager: Village Pharma, LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated November 29, 2023
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- DRUG FACTS:
- ACTIVE INGREDIENTS:
- USES:
- WARNINGS:
-
DIRECTIONS (Adults and Children Over 12 Years):
Clean and dry affected area.
Remove patch from backing and apply to affected area.
Use only one patch at a time, and maximum of four patches / day.
Leave patch on affected area for up to 8 hours
Do not use patches for longer than five consecutive days,
Children under 12 should consult physician prior to use.
- INACTIVE INGREDIENTS:
- SPL UNCLASSIFIED SECTION
- Package Labeling:
-
INGREDIENTS AND APPEARANCE
LIDOZEN
lidocaine, menthol patchProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:71574-900 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength LIDOCAINE (UNII: 98PI200987) (LIDOCAINE - UNII:98PI200987) LIDOCAINE 40 mg in 1 g MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL 10 mg in 1 g Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) GLYCERIN (UNII: PDC6A3C0OX) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) POLYSORBATE 80 (UNII: 6OZP39ZG8H) TARTARIC ACID (UNII: W4888I119H) DIHYDROXYALUMINUM AMINOACETATE (UNII: DO250MG0W6) METHYLPARABEN (UNII: A2I8C7HI9T) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:71574-900-05 5 in 1 POUCH 09/25/2019 1 1 g in 1 PATCH; Type 2: Prefilled Drug Delivery Device/System (syringe, patch, etc.) Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M017 09/16/2019 Labeler - Village Pharma, LLC (080749749)